RRD-251 hydrochloride
CAS No. 72214-67-6
RRD-251 hydrochloride( RRD251 hydrochloride )
Catalog No. M15762 CAS No. 72214-67-6
RRD-251 hydrochloride is a small molecule disruptor of Rb/Raf-1 interaction, potently and selectively disrupts the Rb/Raf-1 (IC50=77 nM).
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
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Biological Information
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Product NameRRD-251 hydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionRRD-251 hydrochloride is a small molecule disruptor of Rb/Raf-1 interaction, potently and selectively disrupts the Rb/Raf-1 (IC50=77 nM).
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DescriptionRRD-251 hydrochloride is a small molecule disruptor of Rb/Raf-1 interaction, potently and selectively disrupts the Rb/Raf-1 (IC50=77 nM) but not Rb/E2F, Rb/prohibitin, Rb/cyclin E, and Rb/HDAC binding; inhibits Rb to recruit Raf-1 to proliferative promoters and inhibited E2F1-dependent transcriptional activity; inhibits anchorage-dependent and anchorage-independent growth of human cancer cells; significantly inhibits tumor growth in tumors with functional Rb in vivo.
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In VitroRRD-251 (10-50 μM; 24 hours) inhibits melanoma growth in-vitro.RRD-251 (50 μM; 2 hours) inhibits Rb-Raf-1 interaction and Rb phosphorylation in non-small cell lung cancer cells. RRD-251 induces apoptosis (50 μM; 18 hours) and cell cycle arrest (20-50 μM; 4 hours).RRD-251 alters the expression of cell cycle and apoptosis regulatory protein. Cell Proliferation Assay Cell Line:SK-MEL-28 cells , SK-MEL-5 cells, SK-MEL-2 cells Concentration:10 μM, 20 μM, 50 μM Incubation Time:24 hours Result:Inhibited melanoma growth in-vitro.Western Blot AnalysisCell Line:SK-MEL-28 cells , SK-MEL-5 cells, SK-MEL-2 cells Concentration:50 μM Incubation Time:2 hours Result:Showed the depletion of phosphorylated-Rb in RRD-251 treated cells.Apoptosis Analysis Cell Line:SK-MEL-28 cells , SK-MEL-5 cells, SK-MEL-2 cells Concentration:50 μM Incubation Time:18 hours Result:Induced apoptosis.Cell Cycle Analysis Cell Line:SK-MEL-28 cells , SK-MEL-5 cells Concentration:20 μM, 50 μM Incubation Time:4 hours Result:Resulted in a dose dependent inhibition of cell cycle progression in SK-MEL-28 and SK-MEL-5 cells, respectively.
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In VivoRRD-251 (50 mg/kg; i.p.; q.o.d; for 14 days) has anti-cancer activities in vivo on melanomas. Animal Model:8-wk-old female athymic nude mice, with SK-ME-28 xenograft Dosage:50 mg/kg Administration:Intraperitoneal administration, qod, for 14 days Result:Inhibits the growth of SK-ME-28 xenograft in nude mice.
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SynonymsRRD251 hydrochloride
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PathwayMAPK/ERK Signaling
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TargetRaf
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RecptorRaf
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Research Area——
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Indication——
Chemical Information
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CAS Number72214-67-6
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Formula Weight271.584
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Molecular FormulaC8H9Cl3N2S
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 125 mg/mL (460.25 mM)
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SMILESC1=CC(=C(C=C1Cl)Cl)CSC(=N)N.Cl
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Chemical NameCarbamimidothioic acid, (2,4-dichlorophenyl)methyl ester, monohydrochloride (9CI)
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Kinkade R, et al. Cancer Res. 2008 May 15;68(10):3810-8.
2. Singh S, et al. Mol Cancer Ther. 2010 Dec;9(12):3330-41.
3. Trevi?o JG, et al. Mol Cancer Ther. 2013 Dec;12(12):2722-34.
4. Wallace AS, et al. Oncotarget. 2016 Jul 19;7(29):46401-46418.
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